Canonical Allele Identifier: CA992743537
Gene: TBXA2R HGNC NCBI

Linked Data

dbSNP Id: rs528449012

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3595377dup , CM000681.2:g.3595377dup GRCh38
NC_000019.9:g.3595375dup , CM000681.1:g.3595375dup GRCh37
NC_000019.8:g.3546375dup NCBI36
NG_013363.1:g.16457dup , LRG_578:g.16457dup
NG_031943.1:g.14807dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375190.10:c.*311dup MANE Select ENSP00000364336.4:n.*311dup
ENST00000375190.8:c.*311dup ENSP00000364336.3:n.*311dup
ENST00000411851.3:c.984-301dup ENSP00000393333.2:n.984-301dup
ENST00000589966.1:c.*174dup ENSP00000468145.1:n.*174dup
NM_001060.5:c.*311dup , LRG_578t1:c.*311dup NP_001051.1:n.*311dup
NM_201636.2:c.984-301dup NP_963998.2:n.984-301dup
NM_001060.6:c.*311dup MANE Select NP_001051.1:n.*311dup
NM_201636.3:c.984-301dup NP_963998.2:n.984-301dup